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Journal Articles

Identification of a Novel Gene Regulatory Element in Human Erythroid Progenitor Cells

Vincent P Schulz, Kimberly Lezon-Geyda, Peiying Shan, Julien Papoin, Mohandas Narla, Laurie A. Steiner, Lionel Blanc, James Palis, Patrick G Gallagher

Blood (2023) 142 (Supplement 1): 9.

https://doi.org/10.1182/blood-2023-186046

Published: 2023

Journal Articles

Multimodality Platelet Evaluation By Mass Cytometry and Genetic Analysis in Patients with Bleeding Disorders

Sean X Gu, Patrick G Gallagher, Ayesha Butt, Vivian W Gu, Kimberly Lezon-Geyda, Vincent P Schulz, Stephanie Prozora, Alfred I Lee, Natalia Neparidze, Noffar Bar, Kelsey Martin, Jennifer Cornell, Giavanna Chirico, Raja Chakraborty, Henry M Rinder, John Hwa, Robert D Bona

Blood (2023) 142 (Supplement 1): 1197.

https://doi.org/10.1182/blood-2023-177946

Published: 2023

Journal Articles

Regulation of RNA polymerase II activity is essential for terminal erythroid maturation

Zachary C. Murphy, Kristin Murphy, Jacquelyn Myers, Michael Getman, Tyler Couch, Vincent P. Schulz, Kimberly Lezon-Geyda, Cal Palumbo, Hongxia Yan, Narla Mohandas, Patrick G. Gallagher, Laurie A. Steiner

Blood (2021) 138 (18): 1740–1756.

https://doi.org/10.1182/blood.2020009903

Published: 2021

Includes: Supplemental data

Journal Articles

Terminal Erythroid Maturation Is Associated with Dynamic Changes in the Abundance of Histone Marks Associated with Active Transcription Elongation and RNA Polymerase II Pausing

Zachary C. Murphy, PhD, Tyler A Couch, BS, Jacquelyn Lillis, MS, Michael Getman, MS, Kimberly Lezon-Geyda, PhD, Vincent P Schulz, PhD, Mohandas Narla, DSc, Patrick G. Gallagher, MD, Laurie A. Steiner, MD

Blood (2019) 134 (Supplement_1): 154.

https://doi.org/10.1182/blood-2019-129561

Published: 2019

Journal Articles

Pklr Intron Splicing-Associated Mutations and Alternate Diagnoses Are Common in Pyruvate Kinase Deficient Patients with Single or No Pklr Coding Mutations

Kimberly Lezon-Geyda, PhD, Melissa J. Rose, DO, Melissa A. McNaull, MD, Christine M. Knoll, MD, Hassan M. Yaish, MD, Yves D. Pastore, MD, Elisa Fermi, Bertil Glader, MD, Paola Bianchi, BSc, PhD, Rachael F. Grace, MD, Patrick G. Gallagher, MD

Blood (2018) 132 (Supplement 1): 3607.

https://doi.org/10.1182/blood-2018-99-117805

Published: 2018

Journal Articles

Altered Splicing from a Mutated Alternate Branch Point Is Common in Severe Alpha-Spectrin Linked Inherited Anemia

Kimberly Lezon-Geyda, PhD, Vincent P Schulz, PhD, Yelena Maksimova, MS, Patrick G. Gallagher, MD

Blood (2018) 132 (Supplement 1): 503.

https://doi.org/10.1182/blood-2018-99-117752

Published: 2018

Journal Articles

Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study

Blood (2018) 131 (20): 2183–2192.

https://doi.org/10.1182/blood-2017-10-810796

Published: 2018

Includes: Supplemental data

Journal Articles

A Ser725Arg mutation in Band 3 abolishes transport function and leads to anemia and renal tubular acidosis

Elizabeth Yang, Patricia Seo-Mayer, Kimberly Lezon-Geyda, Katherine E. Badior, Jing Li, Joseph R. Casey, Reinhart A. F. Reithmeier, Patrick G. Gallagher

Blood (2018) 131 (15): 1759–1763.

https://doi.org/10.1182/blood-2018-01-827725

Published: 2018

Journal Articles

Genotype-Phenotype Correlation and Molecular Heterogeneity in Pyruvate Kinase Deficiency: Data from the PKD Natural History Study

Paola Bianchi, BSc, PhD, Elisa Fermo, PhD, Kimberly Lezon-Geyda, PhD, Patrick G. Gallagher, MD, Richard van Wijk, PhD, Eduard J. Van Beers, MD, Hassan M. Yaish, MD, Janet L. Kwiatkowski, MD, Peter E. Newburger, MD, Yaddanapudi Ravindranath, MBBS, Oliver Andres, MD, Wilma Barcellini, MD, D. Holmes Morton, MD, Bertil Glader, MD, Stefan W. Eber, MD, Satheesh Chonat, MD, Nina Kollmar, MD, Jenny M. Despotovic, DO, MS, Christine M. Knoll, MD, Kevin H.M. Kuo, MD MSc, FRCPC, Dagmar Pospisilova, Prof. MD PhD, Yves D. Pastore, MD, Alexis A Thompson, MD MPH, Winfred Wang, MD, Marcin W. Wlodarski, MD PhD, Jennifer A. Rothman, MD, Heng Wang, MD PhD, Suzanne Holzhauer, MD MSc, Vicky R. Breakey, BSc,MDFRCPC, Joachim B. Kunz, MD, Sujit Sheth, MD, Mukta Sharma, MD MPH, Melissa J. Rose, DO, Heather A. Bradeen, MD, Melissa N. McNaull, MD, Gabrielle P. Ooyama, Nolan Neu, BS, Hasan Al-Sayegh, Wendy B. London, PhD, Rachael F. Grace, MD

Blood (2017) 130 (Supplement 1): 3479.

https://doi.org/10.1182/blood.V130.Suppl_1.3479.3479

Published: 2017

Journal Articles

Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis

Edyta Glogowska, Eve R. Schneider, Yelena Maksimova, Vincent P. Schulz, Kimberly Lezon-Geyda, John Wu, Kottayam Radhakrishnan, Siobán B. Keel, Donald Mahoney, Alison M. Freidmann, Rachel A. Altura, Elena O. Gracheva, Sviatoslav N. Bagriantsev, Theodosia A. Kalfa, Patrick G. Gallagher

Blood (2017) 130 (16): 1845–1856.

https://doi.org/10.1182/blood-2017-05-786004

Published: 2017

Includes: Multimedia, Supplemental data

Journal Articles

Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants

Blood (2015) 126 (23): 3337.

https://doi.org/10.1182/blood.V126.23.3337.3337

Published: 2015

Journal Articles

Mutations in the Gardos channel ( KCNN4 ) are associated with hereditary xerocytosis

Edyta Glogowska, Kimberly Lezon-Geyda, Yelena Maksimova, Vincent P. Schulz, Patrick G. Gallagher

Blood (2015) 126 (11): 1281–1284.

https://doi.org/10.1182/blood-2015-07-657957

Published: 2015

Journal Articles

Global transcriptome analysis and enhancer landscape of human primary T follicular helper and T effector lymphocytes

Jason S. Weinstein, Kimberly Lezon-Geyda, Yelena Maksimova, Samuel Craft, Yaoping Zhang, Mack Su, Vincent P. Schulz, Joseph Craft, Patrick G. Gallagher

Blood (2014) 124 (25): 3719–3729.

https://doi.org/10.1182/blood-2014-06-582700

Published: 2014

Includes: Supplemental data

Journal Articles

Severe Alpha-Spectrin Linked Recessive Hereditary Spherocytosis

Kimberly Lezon-Geyda, PhD, Yelena Maksimova, MS, Vincent P Schulz, PhD, Bernard G Forget, MD, Patrick G Gallagher, MD

Blood (2014) 124 (21): 4011.

https://doi.org/10.1182/blood.V124.21.4011.4011

Published: 2014

Journal Articles

Enhancers and Super Enhancers Are Associated With Genes That Control Phenotypic Traits In Primary Human Erythroid Cells

Vincent P Schulz, PhD, Kimberly Lezon-Geyda, PhD, Yelena Maksimova, MS, Patrick G Gallagher, MD

Blood (2013) 122 (21): 1200.

https://doi.org/10.1182/blood.V122.21.1200.1200

Published: 2013

Journal Articles

The Patient With Transfusion-Dependent Anemia: Diagnosis and Directed Management With Targeted Next Generation Sequencing and Copy Number Analysis

Vincent P Schulz, PhD, Yelena Maksimova, MS, Kimberly Lezon-Geyda, PhD, Patrick G Gallagher, MD

Blood (2013) 122 (21): 3419.

https://doi.org/10.1182/blood.V122.21.3419.3419

Published: 2013

Journal Articles

PR-domain–containing Mds1-Evi1 is critical for long-term hematopoietic stem cell function

Yi Zhang, Sandra Stehling-Sun, Kimberly Lezon-Geyda, Subhash C. Juneja, Lucie Coillard, Gouri Chatterjee, Charles A. Wuertzer, Fernando Camargo, Archibald S. Perkins

Blood (2011) 118 (14): 3853–3861.

https://doi.org/10.1182/blood-2011-02-334680

Published: 2011

Includes: Supplemental data

Journal Articles

Development of a Novel Polyamide-Based Agent to Inhibit EVI1 Function

Géraldine Sicot, Marion Vogel, Yi Zhang, Daniel A Harki, Ph.D., Kimberly Lezon-Geyda, Ph.D., Peter Dervan, Archibald S. Perkins, MD, PhD

Blood (2008) 112 (11): 2660.

https://doi.org/10.1182/blood.V112.11.2660.2660

Published: 2008

Journal Articles

Analysis of a LacZ Knock-In Allele of MDS1 Indicates a Critical Role in Hematopoietic Development.

Archibald S. Perkins, MD, PhD, Sharon Lin, Jacob delCampo, Ph.D., Fernando Camargo, Ph.D., Kimberly Lezon-Geyda, Ph.D.

Blood (2006) 108 (11): 444.

https://doi.org/10.1182/blood.V108.11.444.444

Published: 2006

Journal Articles

Role of EVI1 in Cell Cycle Regulation: Relevance of Specific Target Genes.

Archibald S. Perkins, MD, PhD, Ying-Yi Xiao, PhD, Kimberly Lezon-Geyda, PhD, Sharon Lin, Fernando Camargo, PhD, David Tuck, MD, Bogdan Yatsula, PhD

Blood (2005) 106 (11): 1614.

https://doi.org/10.1182/blood.V106.11.1614.1614

Published: 2005

NARROW

Identification of a Novel Gene Regulatory Element in Human Erythroid Progenitor Cells

Multimodality Platelet Evaluation By Mass Cytometry and Genetic Analysis in Patients with Bleeding Disorders

Regulation of RNA polymerase II activity is essential for terminal erythroid maturation

Terminal Erythroid Maturation Is Associated with Dynamic Changes in the Abundance of Histone Marks Associated with Active Transcription Elongation and RNA Polymerase II Pausing

Pklr Intron Splicing-Associated Mutations and Alternate Diagnoses Are Common in Pyruvate Kinase Deficient Patients with Single or No Pklr Coding Mutations

Altered Splicing from a Mutated Alternate Branch Point Is Common in Severe Alpha-Spectrin Linked Inherited Anemia

Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study

A Ser725Arg mutation in Band 3 abolishes transport function and leads to anemia and renal tubular acidosis

Genotype-Phenotype Correlation and Molecular Heterogeneity in Pyruvate Kinase Deficiency: Data from the PKD Natural History Study

Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis

Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants

Mutations in the Gardos channel ( KCNN4 ) are associated with hereditary xerocytosis

Global transcriptome analysis and enhancer landscape of human primary T follicular helper and T effector lymphocytes

Severe Alpha-Spectrin Linked Recessive Hereditary Spherocytosis

Enhancers and Super Enhancers Are Associated With Genes That Control Phenotypic Traits In Primary Human Erythroid Cells

The Patient With Transfusion-Dependent Anemia: Diagnosis and Directed Management With Targeted Next Generation Sequencing and Copy Number Analysis

PR-domain–containing Mds1-Evi1 is critical for long-term hematopoietic stem cell function

Development of a Novel Polyamide-Based Agent to Inhibit EVI1 Function

Analysis of a LacZ Knock-In Allele of MDS1 Indicates a Critical Role in Hematopoietic Development.

Role of EVI1 in Cell Cycle Regulation: Relevance of Specific Target Genes.

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American Society of Hematology

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American Society of Hematology

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